Manufacturing Associate Level III

Lonza•Portsmouth, NH

1d•Onsite

About The Position

As a Biotechnologist III at our Portsmouth site, you will play a key role in upstream production of therapeutic proteins that support patients worldwide. You will operate manufacturing equipment, execute complex processes, and ensure all work meets cGMP and safety standards. This is an onsite role requiring hands-on work and close collaboration. You will also support troubleshooting, lead by example within the team, and contribute to continuous improvement initiatives. This role follows a 12-hour day shift schedule from 7:00 AM to 7:00 PM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).

Requirements

3+ years of upstream bioprocessing experience required
Experience in GMP manufacturing or a regulated biopharmaceutical environment
Strong understanding of cGMP, documentation practices, and process flow
Ability to troubleshoot equipment and support investigations
Strong communication skills, including technical writing
Attention to detail with strong problem-solving and decision-making skills
High school diploma or equivalent required

Nice To Haves

5+ years in the biotech industry preferred
Associate’s or Bachelor’s degree in a science-related field preferred

Responsibilities

Set up, operate, and monitor manufacturing equipment, including CIP and SIP processes
Execute production processes following SOPs, cGMP, and GDP requirements
Perform advanced laboratory tasks such as sampling, pH, and conductivity testing
Troubleshoot routine and non-routine equipment and process issues
Review batch records, logbooks, and support deviation initiation
Train and support other associates on manufacturing tasks and process knowledge
Perform material movements and maintain equipment through cleaning and sanitization